An atypical Leber's hereditary optic neuropathy with the 11778 mutation.

Author:

Hotta Y,Hayakawa M,Fujiki K,Shinohara K,Sado K,Kanai A,Yanashima K

Publisher

BMJ

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference7 articles.

1. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy;Wallace, D.C.; Singh, G.; Lott, M.T.; Hodge, J.A.; Shurr, T.G.; Lezza, A.M.S.;Science,1988

2. Leber hereditary optic neuropathy: involvement of the mitochondrial NDI gene and evidence for an intragenic suppressor mutation;Howell, N.; Kubacka, I.; Xu, M.; McCullough, D.A.;AmJ Hwn Genet,1991

3. A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy;Huoponen, K.; Vilkki, J.; Aula, P.; Nikoskelainen, E.K.; Savontaus, M.-L.;Am J Hum Genet,1991

4. Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy;Brown, M.D.; Voljavec, A.S.; Lott, M.T.; Torroni, A.; Yang, C.-C.; WaLace, D.C.;Genetics,1992

5. A high frequency of mitochondrial ND4 gene mutation in Japanese pedigrees with Leber hereditary optic neuropathy;Nakamura, M.; Ara, F.; Yamada, M.; Hotta, Y.; Hayakawa, M.; Fujiki, K.;JpnJ Ophthalmol,1992

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